Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C30H38N4O4.C6H6O3S |
Molecular Weight | 676.822 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OS(=O)(=O)C1=CC=CC=C1.[H][C@]2([C@@H](C)CC)N([C@@H](C(=O)N3CCOCC3)C4=CC=C(C)N=C4C)C(=O)[C@H](NC2=O)C5CC6=C(C5)C=CC=C6
InChI
InChIKey=BEWUOCYETMDWGE-FKDQZALLSA-N
InChI=1S/C30H38N4O4.C6H6O3S/c1-5-18(2)26-28(35)32-25(23-16-21-8-6-7-9-22(21)17-23)29(36)34(26)27(24-11-10-19(3)31-20(24)4)30(37)33-12-14-38-15-13-33;7-10(8,9)6-4-2-1-3-5-6/h6-11,18,23,25-27H,5,12-17H2,1-4H3,(H,32,35);1-5H,(H,7,8,9)/t18-,25+,26+,27+;/m0./s1
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P30559 Gene ID: 5021.0 Gene Symbol: OXTR Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/22239250 |
9.9 null [pKi] |
PubMed
Title | Date | PubMed |
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Pyridyl-2,5-diketopiperazines as potent, selective, and orally bioavailable oxytocin antagonists: synthesis, pharmacokinetics, and in vivo potency. | 2012 Jan 26 |
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Inhibition of ejaculation by the non-peptide oxytocin receptor antagonist GSK557296: a multi-level site of action. | 2013 Aug |
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Single- and Multiple-Day Dosing Studies to Investigate High-Dose Pharmacokinetics of Epelsiban and Its Metabolite, GSK2395448, in Healthy Female Volunteers. | 2018 Jan |
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NCI_THESAURUS |
C98292
Created by
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H629P9T4UN
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XX-153
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C99152
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300000041363
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1159097-48-9
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51352566
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CHEMBL2037511
Created by
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ACTIVE MOIETY
SUBSTANCE RECORD